UP AND UP ANTIBIOTIC PLUS PAIN RELIEF (NEOMYCIN, POLYMYXIN B, PRAMOXINE HCL) CREAM [TARGET CORPORATION]

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UP AND UP ANTIBIOTIC PLUS PAIN RELIEF (NEOMYCIN, POLYMYXIN B, PRAMOXINE HCL) CREAM [TARGET CORPORATION]
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NDC 11673-313-58, 11673-313-64
Set ID 532ad823-0168-478e-9c63-83a54797657a
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class Aminoglycoside Antibacterial
Product Number
Application Number PART333B
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  • Active ingredients (in each gram)

    Neomycin sulfate equivalent to 3.5 mg of neomycin base

    Polymyxin B 10,000 units as polymyxin B sulfate

    Pramoxine HCl 10 mg

  • Purpose

    First aid antibiotic

    External analgesic

  • Uses

    first aid to help prevent infection and for temporary relief of pain or discomfort in minor:

    •
    cuts
    •
    scrape
    •
    burns
  • Warnings

    For external use only.

    Do not use

    •
    if you are allergic to any of the ingredients
    •
    in the eyes
    •
    over large areas of the body

    Ask a doctor before use if you have

    •
    deep or puncture wounds
    •
    animal bites
    •
    serious burns

    Stop use and ask a doctor if

    •
    you need to use longer than 1 week
    •
    condition persists or gets worse
    •
    symptoms persist for more than 1 week, or clear up and occur again within a few days
    •
    rash or other allergic reaction develops

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

  • Directions

    •
    adults and children 2 years of age or older:
    •
    clean the affected area
    •
    apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
    •
    may be covered with a sterile bandage
    •
    children under 2 years of age: ask a doctor
  • Other information

    •
    store at 20°-25°C (68°-77°F)
  • Inactive ingredients

    emulsifying wax, methylparaben, mineral oil, poloxamer 188, propylene glycol, purified water, white petrolatum

  • Questions?

    Call 1-888-547-7400

  • Principal Display Panel

    Compare to active ingredients in Neosporin® + Pain Relief

    maximum strength

    antibiotic cream + pain relief

    first aid antibiotic/pain-relieving cream

    Compare to active ingredients in Neosporin® + Pain Relief

    maximum strength

    antibiotic cream + pain relief

    first aid antibiotic/pain-relieving cream

    #1 doctor recommended combination of active ingredients

    neomycin sulfate/polymyxin B sulfate/pramoxine HCl

    soothing infection protection for burns, cuts and scrapes

    NET WT .5 OZ (14 g)

    Antibiotic Cream + Pain Relief Carton
  • INGREDIENTS AND APPEARANCE
    UP AND UP ANTIBIOTIC PLUS PAIN RELIEF 
    neomycin, polymyxin b, pramoxine hcl cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-313
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLOXAMER 188 (UNII: LQA7B6G8JG)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-313-641 in 1 CARTON04/09/2015
    128 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:11673-313-581 in 1 CARTON04/09/2015
    214 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B04/09/2015
    Labeler - Target Corporation (006961700)
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